Intraoperative neurophysiology in deep brain surgery for psychogenic dystonia
Identifieur interne : 000003 ( Pmc/Corpus ); précédent : 000002; suivant : 000004Intraoperative neurophysiology in deep brain surgery for psychogenic dystonia
Auteurs : Vesper Fe Marie L. Ramos ; Ajay S. Pillai ; Codrin Lungu ; Jill Ostrem ; Philip Starr ; Mark HallettSource :
- Annals of Clinical and Translational Neurology [ 2328-9503 ] ; 2015.
Abstract
Psychogenic dystonia is a challenging entity to diagnose and treat because little is known about its pathophysiology. We describe two cases of psychogenic dystonia who underwent deep brain stimulation when thought to have organic dystonia. The intraoperative microelectrode recordings in globus pallidus internus were retrospectively compared with those of five patients with known DYT1 dystonia using spontaneous discharge parameters of rate and bursting, as well as movement-related discharges. Our data suggest that simple intraoperative neurophysiology measures in single subjects do not differentiate psychogenic dystonia from DYT1 dystonia.
Url:
DOI: 10.1002/acn3.206
PubMed: 26125045
PubMed Central: 4479530
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Intraoperative neurophysiology in deep brain surgery for psychogenic dystonia</title><author><name sortKey="Ramos, Vesper Fe Marie L" sort="Ramos, Vesper Fe Marie L" uniqKey="Ramos V" first="Vesper Fe Marie L" last="Ramos">Vesper Fe Marie L. Ramos</name><affiliation><nlm:aff id="au1"><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author><author><name sortKey="Pillai, Ajay S" sort="Pillai, Ajay S" uniqKey="Pillai A" first="Ajay S" last="Pillai">Ajay S. Pillai</name><affiliation><nlm:aff id="au1"><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author><author><name sortKey="Lungu, Codrin" sort="Lungu, Codrin" uniqKey="Lungu C" first="Codrin" last="Lungu">Codrin Lungu</name><affiliation><nlm:aff id="au2"><institution>Parkinson Clinic, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author><author><name sortKey="Ostrem, Jill" sort="Ostrem, Jill" uniqKey="Ostrem J" first="Jill" last="Ostrem">Jill Ostrem</name><affiliation><nlm:aff id="au3"><institution>Surgical Movement Disorders Center, UCSF</institution><addr-line>San Francisco, California, 94115</addr-line></nlm:aff></affiliation></author><author><name sortKey="Starr, Philip" sort="Starr, Philip" uniqKey="Starr P" first="Philip" last="Starr">Philip Starr</name><affiliation><nlm:aff id="au4"><institution>Neurological Surgery, UCSF</institution><addr-line>San Francisco, California, 94143</addr-line></nlm:aff></affiliation></author><author><name sortKey="Hallett, Mark" sort="Hallett, Mark" uniqKey="Hallett M" first="Mark" last="Hallett">Mark Hallett</name><affiliation><nlm:aff id="au1"><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">26125045</idno><idno type="pmc">4479530</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479530</idno><idno type="RBID">PMC:4479530</idno><idno type="doi">10.1002/acn3.206</idno><date when="2015">2015</date><idno type="wicri:Area/Pmc/Corpus">000003</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000003</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Intraoperative neurophysiology in deep brain surgery for psychogenic dystonia</title><author><name sortKey="Ramos, Vesper Fe Marie L" sort="Ramos, Vesper Fe Marie L" uniqKey="Ramos V" first="Vesper Fe Marie L" last="Ramos">Vesper Fe Marie L. Ramos</name><affiliation><nlm:aff id="au1"><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author><author><name sortKey="Pillai, Ajay S" sort="Pillai, Ajay S" uniqKey="Pillai A" first="Ajay S" last="Pillai">Ajay S. Pillai</name><affiliation><nlm:aff id="au1"><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author><author><name sortKey="Lungu, Codrin" sort="Lungu, Codrin" uniqKey="Lungu C" first="Codrin" last="Lungu">Codrin Lungu</name><affiliation><nlm:aff id="au2"><institution>Parkinson Clinic, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author><author><name sortKey="Ostrem, Jill" sort="Ostrem, Jill" uniqKey="Ostrem J" first="Jill" last="Ostrem">Jill Ostrem</name><affiliation><nlm:aff id="au3"><institution>Surgical Movement Disorders Center, UCSF</institution><addr-line>San Francisco, California, 94115</addr-line></nlm:aff></affiliation></author><author><name sortKey="Starr, Philip" sort="Starr, Philip" uniqKey="Starr P" first="Philip" last="Starr">Philip Starr</name><affiliation><nlm:aff id="au4"><institution>Neurological Surgery, UCSF</institution><addr-line>San Francisco, California, 94143</addr-line></nlm:aff></affiliation></author><author><name sortKey="Hallett, Mark" sort="Hallett, Mark" uniqKey="Hallett M" first="Mark" last="Hallett">Mark Hallett</name><affiliation><nlm:aff id="au1"><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></nlm:aff></affiliation></author></analytic><series><title level="j">Annals of Clinical and Translational Neurology</title><idno type="ISSN">2328-9503</idno><idno type="eISSN">2328-9503</idno><imprint><date when="2015">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Psychogenic dystonia is a challenging entity to diagnose and treat because little is known about its pathophysiology. We describe two cases of psychogenic dystonia who underwent deep brain stimulation when thought to have organic dystonia. The intraoperative microelectrode recordings in globus pallidus internus were retrospectively compared with those of five patients with known DYT1 dystonia using spontaneous discharge parameters of rate and bursting, as well as movement-related discharges. Our data suggest that simple intraoperative neurophysiology measures in single subjects do not differentiate psychogenic dystonia from DYT1 dystonia.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Ostrem, Jl" uniqKey="Ostrem J">JL Ostrem</name></author><author><name sortKey="Starr, Pa" uniqKey="Starr P">PA Starr</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Volkmann, J" uniqKey="Volkmann J">J Volkmann</name></author><author><name sortKey="Wolters, A" uniqKey="Wolters A">A Wolters</name></author><author><name sortKey="Kupsch, A" uniqKey="Kupsch A">A Kupsch</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Starr, Pa" uniqKey="Starr P">PA Starr</name></author><author><name sortKey="Rau, Gm" uniqKey="Rau G">GM Rau</name></author><author><name sortKey="Davis, V" uniqKey="Davis V">V Davis</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Hutchison, Wd" uniqKey="Hutchison W">WD Hutchison</name></author><author><name sortKey="Lang, Ae" uniqKey="Lang A">AE Lang</name></author><author><name sortKey="Dostrovsky, Jo" uniqKey="Dostrovsky J">JO Dostrovsky</name></author><author><name sortKey="Lozano, Am" uniqKey="Lozano A">AM Lozano</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Legendy, Cr" uniqKey="Legendy C">CR Legendy</name></author><author><name sortKey="Salcman, M" uniqKey="Salcman M">M Salcman</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kobayashi, K" uniqKey="Kobayashi K">K Kobayashi</name></author><author><name sortKey="Lang, Ae" uniqKey="Lang A">AE Lang</name></author><author><name sortKey="Hallett, M" uniqKey="Hallett M">M Hallett</name></author><author><name sortKey="Lenz, Fa" uniqKey="Lenz F">FA Lenz</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Vitek, Jl" uniqKey="Vitek J">JL Vitek</name></author><author><name sortKey="Chockkan, V" uniqKey="Chockkan V">V Chockkan</name></author><author><name sortKey="Zhang, Jy" uniqKey="Zhang J">JY Zhang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tang, Jk" uniqKey="Tang J">JK Tang</name></author><author><name sortKey="Moro, E" uniqKey="Moro E">E Moro</name></author><author><name sortKey="Mahant, N" uniqKey="Mahant N">N Mahant</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Vitek, Jl" uniqKey="Vitek J">JL Vitek</name></author><author><name sortKey="Delong, Mr" uniqKey="Delong M">MR Delong</name></author><author><name sortKey="Starr, Pa" uniqKey="Starr P">PA Starr</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Vitek, Jl" uniqKey="Vitek J">JL Vitek</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="brief-report"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Ann Clin Transl Neurol</journal-id><journal-id journal-id-type="iso-abbrev">Ann Clin Transl Neurol</journal-id><journal-id journal-id-type="publisher-id">acn3</journal-id><journal-title-group><journal-title>Annals of Clinical and Translational Neurology</journal-title></journal-title-group><issn pub-type="ppub">2328-9503</issn><issn pub-type="epub">2328-9503</issn><publisher><publisher-name>John Wiley & Sons, Ltd</publisher-name><publisher-loc>Chichester, UK</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">26125045</article-id><article-id pub-id-type="pmc">4479530</article-id><article-id pub-id-type="doi">10.1002/acn3.206</article-id><article-categories><subj-group subj-group-type="heading"><subject>Brief Communications</subject></subj-group></article-categories><title-group><article-title>Intraoperative neurophysiology in deep brain surgery for psychogenic dystonia</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Ramos</surname><given-names>Vesper Fe Marie L</given-names></name><xref ref-type="aff" rid="au1">1</xref><xref ref-type="corresp" rid="cor1"></xref></contrib><contrib contrib-type="author"><name><surname>Pillai</surname><given-names>Ajay S</given-names></name><xref ref-type="aff" rid="au1">1</xref></contrib><contrib contrib-type="author"><name><surname>Lungu</surname><given-names>Codrin</given-names></name><xref ref-type="aff" rid="au2">2</xref></contrib><contrib contrib-type="author"><name><surname>Ostrem</surname><given-names>Jill</given-names></name><xref ref-type="aff" rid="au3">3</xref></contrib><contrib contrib-type="author"><name><surname>Starr</surname><given-names>Philip</given-names></name><xref ref-type="aff" rid="au4">4</xref></contrib><contrib contrib-type="author"><name><surname>Hallett</surname><given-names>Mark</given-names></name><xref ref-type="aff" rid="au1">1</xref></contrib><aff id="au1"><label>1</label><institution>Human Motor Control, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></aff><aff id="au2"><label>2</label><institution>Parkinson Clinic, NIH-NINDS</institution><addr-line>Bethesda, Maryland, 20814</addr-line></aff><aff id="au3"><label>3</label><institution>Surgical Movement Disorders Center, UCSF</institution><addr-line>San Francisco, California, 94115</addr-line></aff><aff id="au4"><label>4</label><institution>Neurological Surgery, UCSF</institution><addr-line>San Francisco, California, 94143</addr-line></aff></contrib-group><author-notes><corresp id="cor1"><bold>Correspondence</bold> Vesper Fe Marie Llaneza Ramos, Human Motor Control Section, National Institutes of Health, Building 10, Room 7D42, 10 Center Drive, Bethesda, MD 20814. Tel: 301 4023496; Fax: 301 4802286; E-mail: <email>vesper.ramos@yahoo.com</email></corresp><fn><p><bold>Funding Information</bold> This work was supported by the NINDS Intramural Program.</p></fn></author-notes><pub-date pub-type="ppub"><month>6</month><year>2015</year></pub-date><pub-date pub-type="epub"><day>17</day><month>4</month><year>2015</year></pub-date><volume>2</volume><issue>6</issue><fpage>707</fpage><lpage>710</lpage><history><date date-type="received"><day>23</day><month>3</month><year>2015</year></date><date date-type="accepted"><day>30</day><month>3</month><year>2015</year></date></history><permissions><copyright-statement>© 2015 The Authors. <italic>Annals of Clinical and Translational Neurology</italic> published by Wiley Periodicals, Inc on behalf of American Neurological Association.</copyright-statement><copyright-year>2015</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/"><license-p>This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.</license-p></license></permissions><abstract><p>Psychogenic dystonia is a challenging entity to diagnose and treat because little is known about its pathophysiology. We describe two cases of psychogenic dystonia who underwent deep brain stimulation when thought to have organic dystonia. The intraoperative microelectrode recordings in globus pallidus internus were retrospectively compared with those of five patients with known DYT1 dystonia using spontaneous discharge parameters of rate and bursting, as well as movement-related discharges. Our data suggest that simple intraoperative neurophysiology measures in single subjects do not differentiate psychogenic dystonia from DYT1 dystonia.</p></abstract></article-meta></front><body><sec><title>Introduction</title><p>Psychogenic dystonia is a challenging entity to diagnose and treat, because its pathophysiology is little understood, and separation from organic dystonia has been difficult. Deep brain stimulation (DBS) in the globus pallidus internus (GPi) is an established therapy for generalized dystonia, where better outcomes are associated with earlier treatment.<xref rid="b1" ref-type="bibr">1</xref>,<xref rid="b2" ref-type="bibr">2</xref></p></sec><sec sec-type="methods"><title>Methods</title><p>We describe two patients with psychogenic dystonia who were originally thought to have organic dystonia. Intraoperative microelectrode recordings in GPi in these patients (ages 18 and 23) were retrospectively compared with those from five patients with known DYT1 dystonia (ages 15, 17, 23, 24, and 27) using spontaneous discharge parameters of rate and bursting, as well as movement-related discharges, similar to previous reports.<xref rid="b3" ref-type="bibr">3</xref> Single unit recordings in the GPi were obtained from patients undergoing physiologic mapping for placement of DBS electrodes. All patients received propofol for frame placement and drilling but stopped 30 min prior to recording. Neurons were screened for movement-related activity based on audible changes in action potential discharge evoked by passive (investigator-initiated) limb movements around the shoulder, elbow, wrist, hip, knee, and ankle joints). Two-tailed independent <italic>t</italic>-test analysis was used to explore the differences.</p><sec><title>Case 1: PSY-DYS 1</title><p>A woman had sudden onset of left hand tremor while on a camping trip at age 16. Tremor spontaneously resolved after several months. One year later, she had intermittent stuttering that also went away after a few months, followed by left leg shaking. Two weeks later, she developed painful, symmetric, fairly fixed bilateral inward turning of both feet with toe curling; present when supine or sitting, but worse when standing. She became wheelchair-bound in a few months. She also had a mild symmetric bilateral hand postural tremor. Magnetic resonance imaging brain and whole spine, electroencephalogram, electromyography, DYT1, autoimmune and mitochondrial disease work-up were normal. Botulinum toxin and levodopa gave minimum benefit. At age 18, she was implanted with bilateral GPi DBS. Six weeks postop, on the day of initial programming, she had remarkable improvement in her dystonia and tremor and was able to walk. Improvement persisted and she was able to walk across the stage for her high school graduation and dance at her wedding. Occasionally, she would experience pain and foot inversion that responded to increasing DBS voltage. She remained well for ∼4 years, until she had sudden onset cramping and inward turning of her left foot while attending a crowded concert. The next day, her feet turned inward with toe curling, forcing her to stop driving. Despite adjustment of DBS settings, her symptoms worsened, and she began needing the wheelchair again. She was unable to continue at her job as a perinatal technician. Her programming neurologist noted that blinded changes in her stimulator (including turning the stimulator on and off) did not alter her symptoms. She was diagnosed with psychogenic dystonia, underwent intensive cognitive, and behavioral therapy, and physical therapy. She was successfully explanted and remains symptom-free at age 23.</p></sec><sec><title>Case 2: PSY-DYS2</title><p>A woman, at age 12, had sudden onset tightness in shoulders and neck, more on the right, after being hit by a car and knocked briefly unconscious. She then developed right jaw pulling, right shoulder elevation, and truncal dystonia. Symptoms worsened with not only writing and typing tasks but also progressively worsened with trouble breathing and slurred speech. Magnetic resonance imaging brain and cervical spine, DYT1, and PNKD gene testing were normal. Symptoms were initially controlled by trihexiphenidyl, but could not be continued because of worsening eczema with concern for drug rash. She tried valproate, baclofen, clonazepam, botulinum toxin, and levodopa with no benefit. At age 23, she was implanted with bilateral GPi DBS. Six weeks after initial programming, her torso was much straighter and she had less neck and jaw pulling. After a brief initial improvement, her symptoms worsened with no effect after multiple adjustments to her stimulation parameters. She then developed laryngeal-spasm-like symptoms that were not seen on fiberoptic laryngoscopy. She began having choreiform movements in hands and toe curling with heel tapping. She was hospitalized for depression and suicide attempts with conversion disorder. At age 25, she was diagnosed with psychogenic dystonia and her DBS was turned off. Her symptoms did not worsen. She began to improve with intensive psychiatric, cognitive behavioral, and physical therapy. She was explanted at age 27, being treated with quetiapine and trihexiphenidyl, and she remains symptom-free with occasional flares with stressful situations.</p></sec></sec><sec sec-type="results"><title>Results</title><p>The number of units recorded in each condition was five at rest and 11 with movement for the first psychogenic patient, and three at rest and three with movement for the second psychogenic patient. For the DYT1 dystonia patients, the first patient had 20 units at rest and five with movement, the second had 10 units at rest and five with movement, the third had four units at rest and seven with movement, the fourth had six units at rest, and five with movement, and the fifth had one unit at rest and 13 with movement. Mean rate of firing for the two psychogenic patients were 54.62 and 39.96 Hz, respectively, at rest, and 60.00 and 51.91 Hz, respectively, with passive movement. These were not different from those of the DYT1 patients, with a mean of 56.95 (range: 39.07–81.52) Hz at rest and 56.42 (range 48.52–59.53) with movement (Table<xref ref-type="table" rid="tbl1">1</xref>). Bursting properties for the psychogenic patients showed burst indices<xref rid="b4" ref-type="bibr">4</xref> (2.76 and 6.63 at rest, 2.62 and 1.61 with movement), and proportion of spikes in burst<xref rid="b5" ref-type="bibr">5</xref> (0.07 and 0.36 at rest, 0.06 and 0.02 with movement). These also did not differ significantly from DYT1 patients (burst index mean 3.64 at rest, and 3.17 with movement, mean proportion of spikes in burst 0.11 at rest and 0.07 with movement). Two-tailed independent <italic>t</italic>-tests showed no significant differences. These results are comparatively illustrated in Figure<xref ref-type="fig" rid="fig01">1</xref>.</p><table-wrap id="tbl1" position="float"><label>Table 1</label><caption><p>Electrophysiological characteristics of globus pallidus internus neurons in psychogenic versus DYT-1 dystonia</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left" rowspan="1" colspan="1">Patient</th><th align="left" rowspan="1" colspan="1">Mean firing rate, Hz, at rest (with movement)</th><th align="left" rowspan="1" colspan="1">Interspike interval mean, msec, at rest (with movement)</th><th align="left" rowspan="1" colspan="1">Interspike interval standard deviation, msec, at rest (with movement)</th><th align="left" rowspan="1" colspan="1">Burst index at rest (with movement)</th><th align="left" rowspan="1" colspan="1">Mean firing rate in burst, Hz, at rest (with movement)</th><th align="left" rowspan="1" colspan="1">Mean proportion of spikes in burst at rest (with movement)</th></tr></thead><tbody><tr><td align="left" rowspan="1" colspan="1">PSY-DYS1</td><td align="left" rowspan="1" colspan="1">54.62 (60)</td><td align="left" rowspan="1" colspan="1">19 (18.83)</td><td align="left" rowspan="1" colspan="1">19.33 (18.11)</td><td align="left" rowspan="1" colspan="1">2.76 (2.62)</td><td align="left" rowspan="1" colspan="1">179.10 (187.74)</td><td align="left" rowspan="1" colspan="1">0.07 (0.06)</td></tr><tr><td align="left" rowspan="1" colspan="1">PSY-DYS2</td><td align="left" rowspan="1" colspan="1">39.96 (51.91)</td><td align="left" rowspan="1" colspan="1">40.05 (19.29)</td><td align="left" rowspan="1" colspan="1">67.45 (16.91)</td><td align="left" rowspan="1" colspan="1">6.63 (1.61)</td><td align="left" rowspan="1" colspan="1">115.44 (126.29)</td><td align="left" rowspan="1" colspan="1">0.36 (0.02)</td></tr><tr><td align="left" rowspan="1" colspan="1">DYT 1</td><td align="left" rowspan="1" colspan="1">56.95 (56.42)</td><td align="left" rowspan="1" colspan="1">20.97 (19.54)</td><td align="left" rowspan="1" colspan="1">21.66 (20.32)</td><td align="left" rowspan="1" colspan="1">3.64 (3.17)</td><td align="left" rowspan="1" colspan="1">187.24 (191.77)</td><td align="left" rowspan="1" colspan="1">0.11 (0.07)</td></tr><tr><td align="left" rowspan="1" colspan="1"><italic>t</italic>-test PSY-DYS versus DYT1</td><td align="left" rowspan="1" colspan="1">0.41 (0.93)</td><td align="left" rowspan="1" colspan="1">0.56 (0.64)</td><td align="left" rowspan="1" colspan="1">0.53 (0.2)</td><td align="left" rowspan="1" colspan="1">0.68 (0.24)</td><td align="left" rowspan="1" colspan="1">0.43 (0.46)</td><td align="left" rowspan="1" colspan="1">0.58 (0.26)</td></tr></tbody></table></table-wrap><fig id="fig01" position="float"><label>Figure 1</label><caption><p>Comparative illustration of electrophysiological characteristics of globus pallidus internus (GPi) neurons in psychogenic versus DYT-1 dystonia.</p></caption><graphic xlink:href="acn30002-0707-f1"></graphic></fig></sec><sec sec-type="discussion"><title>Discussion</title><p>Similar to a prior study examining thalamic activity, GPi single unit discharge characteristics do not appear to separate psychogenic dystonia and organic dystonia.<xref rid="b6" ref-type="bibr">6</xref> Previous studies showed lower firing rates for GPi neurons in dystonia versus Parkinson’s disease patients.<xref rid="b3" ref-type="bibr">3</xref>,<xref rid="b7" ref-type="bibr">7</xref>,<xref rid="b8" ref-type="bibr">8</xref> More recently, analysis of pallidal firing rates showed no significant difference between hemidystonia and generalized dystonia patients and Parkinson’s disease patients. The study also showed GPi firing rates did not correlate with dystonia severity.<xref rid="b4" ref-type="bibr">4</xref>,<xref rid="b9" ref-type="bibr">9</xref> For our cohort, all patients underwent surgery at the same institution with the same surgeon. Recordings were obtained uniformly. Microelectrode recordings may be affected by anesthetics,<xref rid="b4" ref-type="bibr">4</xref>,<xref rid="b9" ref-type="bibr">9</xref>,<xref rid="b10" ref-type="bibr">10</xref> but all our patients were studied in the awake state at least 30 min after stopping propofol. Age at the time of surgery and recording was also similar between the DYT1 and psychogenic patients in our study.</p><p>As previously suggested, baseline rates and patterns of neuronal activity need to be compared across fairly large numbers of dystonia cases to draw conclusions concerning the relationship between mean firing rates, response to somatosensory input, or patterns of neural activity in GPi, and the phenotype, or etiology of dystonia.<xref rid="b10" ref-type="bibr">10</xref> However, opportunities to study such cases are not common. Based on our results, spontaneous single unit discharge characteristics in single subjects do not seem to be sensitive markers to help differentiate organic dystonia from DYT1 dystonia. Although caution must be exercised in interpreting our results, it does highlight that there is still no neurophysiologic parameter, and thus no reliable diagnostic test, capable of differentiating between organic and psychogenic dystonia. As such, the diagnosis remains clinical and can be challenging for complex cases. Other features for future investigation, which may be more helpful, include synchronization of discharges across multiple units, power spectrum analysis, or measures of EMG-coherence. Unfortunately, as this study is performed retrospectively, data for these analyses were not available for our patients.</p></sec></body><back><ack><p>This study was supported by the NINDS Intramural Program. The authors would like to thank Traian Popa, Leslie Markun, Elena Ryapolova, Salman Qasim, and Nathan Ziman for their valuable assistance in the preparation of this manuscript.</p></ack><sec><title>Author Contributions</title><p>Dr. Ramos – study conception and design, data gathering, data analysis, drafting, and editing the manuscript. Dr. Pillai – study conception and design, data analysis, drafting, and editing the manuscript. Dr. Lungu – study conception and design, data gathering, data analysis, drafting, and editing the manuscript. Dr. Ostrem – study conception and design, data gathering, data analysis, and editing the manuscript. Dr. Starr – study conception and design, data gathering, data analysis, editing the manuscript. Dr. Hallett – study conception and design, data analysis, drafting, and editing the manuscript. All authors approved the final draft of the paper being submitted.</p></sec><sec><title>Conflict of Interest</title><p>Dr. Ramos is a federal government employee, working for the National Institutes of Health. This study was undertaken as part of her official duty. Her research at the NIH is supported by the NIH Intramural Program. She was also under a fellowship support grant from the Dystonia Medical Research Foundation. Dr. Pillai is a federal government employee, working for the National Institutes of Health. This study was undertaken as part of his official duty. Dr. Lungu is a federal government employee, working for the National Institutes of Health. This study was undertaken as part of his official duty. Dr. Lungu’s research at the NIH is supported by the NIH Intramural Program. Dr. Ostrem reports receiving compensation from Medtronic Consulting and Educational grant support, MRI Interventions grant support, Abbvie consulting, Merz Educational grant support, and Allergan Speakers Program. Dr. Starr receives compensation from Medtronic Consulting and Educational grant support. Dr. Hallett is a federal government employee, working for the National Institutes of Health. This work was undertaken as part of his official duty. Dr. Hallett’s research at the NIH is largely supported by the NIH Intramural Program. Dr. Hallett serves as Chair of the Medical Advisory Board for and receives honoraria and funding for travel from the Neurotoxin Institute. He may accrue revenue on U.S. Patent #6,780,413 B2 (Issued: 24 August 2004): Immunotoxin (MAB-Ricin) for the treatment of focal movement disorders, and U.S. Patent #7,407,478 (Issued: 5 August 2008): Coil for Magnetic Stimulation and methods for using the same (H-coil); in relation to the latter, he has received license fee payments from the NIH (from Brainsway) for licensing of this patent. He is on the Editorial Board of 22 journals, and received royalties from publishing from Cambridge University Press, Oxford University Press, John Wiley and Sons, Wolters Kluwer, and Elsevier. He has received honoraria for lecturing from Columbia. 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